Simone Lupini , Lúrima Uane Soares Faria , Claudio Augusto Oller do Nascimento , Debora F. Rodrigues
{"title":"在镰刀菌中,菌丝内细菌群落调节真菌对丝球相关细菌的反应","authors":"Simone Lupini , Lúrima Uane Soares Faria , Claudio Augusto Oller do Nascimento , Debora F. Rodrigues","doi":"10.1016/j.funeco.2025.101455","DOIUrl":null,"url":null,"abstract":"<div><div>Fungi and bacteria form complex associations in soil environments, which can impact their symbiotic relationships. While previous studies have examined either endohyphal bacteria or hyphosphere-associated bacterial community interactions with fungi independently, a critical knowledge gap remains related to how hyphosphere-associated bacteria modulate the endohyphal bacterial communities and fungal responses. This study investigated the impact of hyphosphere-associated bacteria co-culture with three <em>Fusarium</em> isolates containing natural endohyphal bacteria (composed primarily of <em>Cutibacterium</em>, <em>Acinetobacter</em>, <em>Pelomonas</em>, <em>Achromobacter</em>, <em>Citrobacter,</em> and other less abundant species) and their antibiotic-treated counterparts with reduced endohyphal bacterial communities. The study determined the changes in fungal growth and microbiome composition when co-cultured with individual or a bacterial mix of four rhizosphere bacterial isolates (<em>Pseudomonas</em>, <em>Bacillus</em>, <em>Stenotrophomonas</em>, and <em>Rhizobium</em>). Results showed that endohyphal bacteria modulated fungal responses to hyphosphere-associated bacteria co-culture, with wild-type fungi typically exhibiting lower growth inhibition than their counterparts with reduced diversity and quantity of endohyphal bacteria. However, when the fungi were exposed to a synthetic hyphosphere-associated bacterial mix, all fungal isolates stimulated the endohyphal bacterial community leading to higher endohyphal bacterial diversity compared to single-species hyphosphere-associated bacterial treatments. These findings highlight the importance of considering complex interactions within the fungal microbiome, demonstrating that endohyphal bacteria respond dynamically to the composition of hyphosphere-associated bacterial communities. Our results also provide new insights into how the interplay between endohyphal and hyphosphere-associated bacterial communities shape fungal biology in soil environments.</div></div>","PeriodicalId":55136,"journal":{"name":"Fungal Ecology","volume":"77 ","pages":"Article 101455"},"PeriodicalIF":2.2000,"publicationDate":"2025-08-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Endohyphal bacterial communities modulate fungal responses to hyphosphere-associated bacteria in Fusarium\",\"authors\":\"Simone Lupini , Lúrima Uane Soares Faria , Claudio Augusto Oller do Nascimento , Debora F. Rodrigues\",\"doi\":\"10.1016/j.funeco.2025.101455\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Fungi and bacteria form complex associations in soil environments, which can impact their symbiotic relationships. While previous studies have examined either endohyphal bacteria or hyphosphere-associated bacterial community interactions with fungi independently, a critical knowledge gap remains related to how hyphosphere-associated bacteria modulate the endohyphal bacterial communities and fungal responses. This study investigated the impact of hyphosphere-associated bacteria co-culture with three <em>Fusarium</em> isolates containing natural endohyphal bacteria (composed primarily of <em>Cutibacterium</em>, <em>Acinetobacter</em>, <em>Pelomonas</em>, <em>Achromobacter</em>, <em>Citrobacter,</em> and other less abundant species) and their antibiotic-treated counterparts with reduced endohyphal bacterial communities. The study determined the changes in fungal growth and microbiome composition when co-cultured with individual or a bacterial mix of four rhizosphere bacterial isolates (<em>Pseudomonas</em>, <em>Bacillus</em>, <em>Stenotrophomonas</em>, and <em>Rhizobium</em>). Results showed that endohyphal bacteria modulated fungal responses to hyphosphere-associated bacteria co-culture, with wild-type fungi typically exhibiting lower growth inhibition than their counterparts with reduced diversity and quantity of endohyphal bacteria. However, when the fungi were exposed to a synthetic hyphosphere-associated bacterial mix, all fungal isolates stimulated the endohyphal bacterial community leading to higher endohyphal bacterial diversity compared to single-species hyphosphere-associated bacterial treatments. These findings highlight the importance of considering complex interactions within the fungal microbiome, demonstrating that endohyphal bacteria respond dynamically to the composition of hyphosphere-associated bacterial communities. Our results also provide new insights into how the interplay between endohyphal and hyphosphere-associated bacterial communities shape fungal biology in soil environments.</div></div>\",\"PeriodicalId\":55136,\"journal\":{\"name\":\"Fungal Ecology\",\"volume\":\"77 \",\"pages\":\"Article 101455\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2025-08-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Fungal Ecology\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1754504825000455\",\"RegionNum\":3,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"ECOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fungal Ecology","FirstCategoryId":"93","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1754504825000455","RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ECOLOGY","Score":null,"Total":0}
Endohyphal bacterial communities modulate fungal responses to hyphosphere-associated bacteria in Fusarium
Fungi and bacteria form complex associations in soil environments, which can impact their symbiotic relationships. While previous studies have examined either endohyphal bacteria or hyphosphere-associated bacterial community interactions with fungi independently, a critical knowledge gap remains related to how hyphosphere-associated bacteria modulate the endohyphal bacterial communities and fungal responses. This study investigated the impact of hyphosphere-associated bacteria co-culture with three Fusarium isolates containing natural endohyphal bacteria (composed primarily of Cutibacterium, Acinetobacter, Pelomonas, Achromobacter, Citrobacter, and other less abundant species) and their antibiotic-treated counterparts with reduced endohyphal bacterial communities. The study determined the changes in fungal growth and microbiome composition when co-cultured with individual or a bacterial mix of four rhizosphere bacterial isolates (Pseudomonas, Bacillus, Stenotrophomonas, and Rhizobium). Results showed that endohyphal bacteria modulated fungal responses to hyphosphere-associated bacteria co-culture, with wild-type fungi typically exhibiting lower growth inhibition than their counterparts with reduced diversity and quantity of endohyphal bacteria. However, when the fungi were exposed to a synthetic hyphosphere-associated bacterial mix, all fungal isolates stimulated the endohyphal bacterial community leading to higher endohyphal bacterial diversity compared to single-species hyphosphere-associated bacterial treatments. These findings highlight the importance of considering complex interactions within the fungal microbiome, demonstrating that endohyphal bacteria respond dynamically to the composition of hyphosphere-associated bacterial communities. Our results also provide new insights into how the interplay between endohyphal and hyphosphere-associated bacterial communities shape fungal biology in soil environments.
期刊介绍:
Fungal Ecology publishes investigations into all aspects of fungal ecology, including the following (not exclusive): population dynamics; adaptation; evolution; role in ecosystem functioning, nutrient cycling, decomposition, carbon allocation; ecophysiology; intra- and inter-specific mycelial interactions, fungus-plant (pathogens, mycorrhizas, lichens, endophytes), fungus-invertebrate and fungus-microbe interaction; genomics and (evolutionary) genetics; conservation and biodiversity; remote sensing; bioremediation and biodegradation; quantitative and computational aspects - modelling, indicators, complexity, informatics. The usual prerequisites for publication will be originality, clarity, and significance as relevant to a better understanding of the ecology of fungi.